Key result
SIRT-1 knockdown blocked autophagy and impeded the non-lytic release of EV-D68, poliovirus, and SARS-CoV-2 in extracellular vesicles.
SIRT-1 is critical for the non-lytic release of enveloped EV-D68, poliovirus, and SARS-CoV-2 viral particles, highlighting a potential host target for broad-spectrum antivirals.
SIRT-1 may represent a host target for broad-spectrum antivirals in animal models; leaves open translation to human viral disease.
Enterovirus D68 is a re-emerging enterovirus that causes acute respiratory illness in infants and has recently been linked to Acute Flaccid Myelitis. Here, we show that the histone deacetylase, SIRT-1, is essential for autophagy and EV-D68 infection. Knockdown of SIRT-1 inhibits autophagy and reduces EV-D68 extracellular titers. The proviral activity of SIRT-1 does not require its deacetylase activity or functional autophagy. SIRT-1’s proviral activity is, we demonstrate, mediated through the repression of ER stress. Inducing ER stress through thapsigargin treatment or SERCA2A knockdown in SIRT-1 knockdown cells had no additional effect on EV-D68 extracellular titers. Knockdown of SIRT-1 also decreases poliovirus and SARS-CoV-2 titers but not coxsackievirus B3. In non-lytic conditions, EV-D68 is primarily released in an enveloped form, and SIRT-1 is required for this process. Our data show that SIRT-1, through its translocation to the cytosol, is critical to promote the release of enveloped EV-D68 viral particles.
No takes yet. Share an insight, caveat, or question.
Jassey et al. (2022) studied Enterovirus D68 infection. SIRT-1 knockdown vs. Scramble control was evaluated on Extracellular viral titers. SIRT-1 knockdown blocked autophagy and impeded the non-lytic release of EV-D68, poliovirus, and SARS-CoV-2 in extracellular vesicles.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: